ClinicalTrials.Veeva

Menu

Tart Cherry and Omega-3's for Aromatase Inhibitor Musculoskeletal Symptoms

P

Philip Chang

Status and phase

Not yet enrolling
Early Phase 1

Conditions

Breast Cancer
Joint Pain
Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS)

Treatments

Drug: Tart Cherry
Drug: Omega 3 FA (Fish Oil)

Study type

Interventional

Funder types

Other

Identifiers

NCT06123286
IIT2022-08-CHANG-TaCO3AIMSS

Details and patient eligibility

About

Both Tart Cherry and Omega 3 FAs have better side effect profiles compared to other commonly used medications for AIMSS, such as nonsteroidal anti-inflammatories, steroids, and serotonin norepinephrine reuptake inhibitors. Additionally, in our clinics we often find that patients tend to be more receptive to taking a supplement as opposed to an additional medication. Further, both Tart Cherry concentrate and fish oil have beneficial properties for helping with joint stiffness in general, in addition to other health issues like insomnia.

There is preliminary evidence in mouse models that when given together, these supplements may have an even greater anti-inflammatory effect than when taken separately14. Although to our knowledge, no human studies have tested this hypothesis. This study has been designed to test the hypothesis that Tart Cherry and fish oil when given in combination over a 12-week period could produce beneficial changes in joint function when compared to Tart Cherry or fish oil in isolation in an obese breast cancer population experiencing AIMSS. Secondary outcomes to be assessed include pain, functional performance, quality of life and cognition.

Enrollment

30 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Breast cancer diagnosis (Stage I-III) with any hormonal status.
  • Females aged ≥ 18 years.
  • Currently receiving AI therapy.
  • BMI ≥ 27.
  • Clinical diagnosis of AIMSS.
  • Omega-3 Index <8%.
  • Average joint pain score ≥ 4 on the Brief Pain Inventory (BPI) within 7 days of enrollment.
  • Written informed consent obtained from subject and ability and willingness of subject to comply with the requirements of the study.

Exclusion criteria

  • Current use of anticoagulant medications (Including but not limited to Warfarin, Lovenox, Eliquis, Xarelto).
  • Allergy to cherries or fish/fish products.
  • Lifetime history of rheumatoid arthritis and/or inflammatory joint diseases (Including but not limited to reactive arthritis, ankylosing spondylitis, and psoriatic arthritis).
  • Uncontrolled diabetes mellitus as determined by treating physician (with or without the use of glucose lowering medications and/or insulin).
  • Lifetime history of stroke or transient ischemic attacks.
  • New use or dose change of oral or topical analgesics in the previous 14 days. (Including but not limited to opioids, non-steroidal anti-inflammatories, acetaminophen, SNRI's, SSRI's, gabapentinoids, tricyclic antidepressants, and muscle relaxants).
  • Oral or intra-articular steroid use in the previous 30 days (Including but not limited to dexamethasone, prednisone, methylprednisolone, triamcinolone, hydrocortisone).
  • History of joint fracture or surgery of the symptomatic joint in the previous 6 months.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Group 1 : Wait list control
No Intervention group
Description:
No supplement but will be offered supplements after finishing the study
Group 2 : Tart Cherry and Omega 3 FA (Fish Oil)
Experimental group
Treatment:
Drug: Omega 3 FA (Fish Oil)
Drug: Tart Cherry

Trial contacts and locations

2

Loading...

Central trial contact

Clinical Trial Navigator

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems